Conditions | Yield |
---|---|
With sodium hydroxide; dihydrogen peroxide | 99% |
With sodium hydroxide; dihydrogen peroxide In water at 15℃; Product distribution / selectivity; | 94% |
With dihydrogen peroxide; potassium hydroxide In water at 5 - 50℃; for 0.0766667h; Flow reactor; | 74.7% |
With sodium peroxide | |
With sodium hydroxide; dihydrogen peroxide |
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical
diisopropyl peroxydicarbonate
1,4-Divinylbenzene
2-(isopropyloxycarbonyloxy)-1-(2',2',6',6'-tetramethyl-1'-piperidinyloxy)-1-(4'-vinylphenyl)ethane
Conditions | Yield |
---|---|
at 55℃; for 5h; | 76.1% |
4-acetoxy-2,2,6,6-tetramethylpiperidine-1-oxyl
diisopropyl peroxydicarbonate
1,4-Divinylbenzene
Conditions | Yield |
---|---|
at 0 - 55℃; for 5h; | 73% |
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical
diisopropyl peroxydicarbonate
1,3-divinylbenzene
Conditions | Yield |
---|---|
70.5% |
4-(benzyloxycarbonyl)-2,2,6,6-tetramethylpiperidine-1-oxyl
diisopropyl peroxydicarbonate
1,4-Divinylbenzene
Conditions | Yield |
---|---|
at 0 - 55℃; for 5h; | 62.1% |
diisopropyl peroxydicarbonate
N-(4-chlorophenylmethylene)-2-methylthiobenzenamine
A
2-(4-chlorophenyl)benzothiazole
B
4-chlorobenzaldehyde
C
(2-aminophenyl)thiomethyl isopropyl carbonate
Conditions | Yield |
---|---|
In benzene at 60℃; for 5h; | A 36% B 48% C 54% |
diisopropyl peroxydicarbonate
1,4-Divinylbenzene
di-tert-butyl nitroxide
Conditions | Yield |
---|---|
at 0 - 55℃; for 5h; | 53.2% |
diisopropyl peroxydicarbonate
benzylidene-(2-methylsulfanyl-phenyl)-amine
A
2-Phenylbenzothiazole
B
benzaldehyde
C
(2-aminophenyl)thiomethyl isopropyl carbonate
Conditions | Yield |
---|---|
In benzene at 60℃; for 5h; | A 17% B 35% C 53% |
diisopropyl peroxydicarbonate
N-(3-nitrophenylmethylene)-2-methylthiobenzenamine
A
2-(3-nitrophenyl)benzothiazole
B
3-nitro-benzaldehyde
C
(2-aminophenyl)thiomethyl isopropyl carbonate
D
<(2-(3-nitrophenyl)methylenamino)phenyl>thiomethyl isopropyl carbonate
Conditions | Yield |
---|---|
With 2,6-di-tert-butylphenol In benzene at 60℃; for 5h; | A 3% B 13% C 10% D 50% |
diisopropyl peroxydicarbonate
[4-(benzylideneamino)phenyl]methanol
A
methyl 6-methoxy-2-phenylquinoline-4-carboxylate
B
carbamic acid, (4-methoxyphenyl)-, 1-methylethyl ester
Conditions | Yield |
---|---|
With acrylic acid methyl ester In benzene at 60℃; for 4h; | A 49% B 14% |
diisopropyl peroxydicarbonate
N-(4-methoxyphenylmethylene)-2-methylthiobenzenamine
A
2-(4-methoxy-phenyl)-benzothiazole
B
4-methoxy-benzaldehyde
C
(2-aminophenyl)thiomethyl isopropyl carbonate
Conditions | Yield |
---|---|
In benzene at 60℃; for 5h; | A 28% B 48% C 39% |
diisopropyl peroxydicarbonate
N-(phenylmethylene)-5-amino-2-methoxypyridine
diethylazodicarboxylate
A
diethyl hydrazodicarboxylate
Conditions | Yield |
---|---|
In benzene at 60℃; | A n/a B n/a C 47% |
diisopropyl peroxydicarbonate
N-(2-thienylmethylene)-2-methylthiobenzenamine
A
thiophene-2-carbaldehyde
B
2-thiophen-2-yl-benzothiazole
C
(2-aminophenyl)thiomethyl isopropyl carbonate
Conditions | Yield |
---|---|
In benzene at 60℃; for 5h; | A 40% B 13% C 45% |
TEMPOL
diisopropyl peroxydicarbonate
1,4-Divinylbenzene
2-(isopropyloxycarbonyloxy)-1-(4'-hydroxy-2',2',6',6'-tetramethyl-1'-piperidinyloxy)-1-(4'-vinylphenyl)ethane
Conditions | Yield |
---|---|
at 0 - 55℃; for 5h; | 41% |
diisopropyl peroxydicarbonate
[4-(benzylideneamino)phenyl]methanol
A
carbamic acid, (4-methoxyphenyl)-, 1-methylethyl ester
Conditions | Yield |
---|---|
With (E)-1,2-diphenyl-ethene In benzene at 60℃; for 4h; | A 15% B 40% C 20% |
diisopropyl peroxydicarbonate
N-(3-nitrophenylmethylene)-2-methylthiobenzenamine
A
2-(3-nitrophenyl)benzothiazole
B
3-nitro-benzaldehyde
C
(2-aminophenyl)thiomethyl isopropyl carbonate
Conditions | Yield |
---|---|
In benzene at 60℃; for 5h; | A 38% B 40% C 35% |
diisopropyl peroxydicarbonate
(E)-N-benzylidenebenzenamine
A
carbamic acid, phenyl-, 1-methylethyl ester
B
2-phenyl-quinoline-3,4-dicarbonitrile
Conditions | Yield |
---|---|
With 1,2-Dicyanoethylene In benzene at 60℃; for 4h; | A 20% B 38% |
diisopropyl peroxydicarbonate
N-(3-phenyl-2-propenylidene)-2-methylthiobenzenamine
A
2-styrylbenzothiazole
B
(2-aminophenyl)thiomethyl isopropyl carbonate
C
3-phenyl-propenal
Conditions | Yield |
---|---|
In benzene at 60℃; for 5h; | A 24% B 30% C 36% |
diisopropyl peroxydicarbonate
diethylazodicarboxylate
A
diethyl hydrazodicarboxylate
Conditions | Yield |
---|---|
In benzene at 60℃; | A n/a B n/a C 36% |
diisopropyl peroxydicarbonate
9-methylene-fluorene
polymer, Mn 1070 by SEC with oligostyrene as standard, Mn 1560 by SEC with oligo(dibenzofulvene) as standard; monomer(s): dibenzofulvene; 2,9-dimethyl-3,5,6,8-tetraoxadeca-4,7-dione
Conditions | Yield |
---|---|
In toluene at 40℃; for 24h; | 33% |
Conditions | Yield |
---|---|
In benzene at 60℃; for 18h; | A 16% B 28% C 11% |
diisopropyl peroxydicarbonate
N-(4-chlorobenzylidene)aniline
A
Isopropyl N-4-chlorophenylcarbamate
Conditions | Yield |
---|---|
With acrylic acid methyl ester In benzene at 60℃; for 4h; | A 27% B 16% |
diisopropyl peroxydicarbonate
N-benzylidene-4-acetylaniline
A
isopropyl (4-acetylphenyl)carbamate
Conditions | Yield |
---|---|
With acrylonitrile In benzene at 60℃; for 4h; | A 23% B 27% |
diisopropyl peroxydicarbonate
A
triphenylmethyl alcohol
B
2-(4-chlorophenyl)benzoxazole
C
triphenylmethyl iso-propyl ether
Conditions | Yield |
---|---|
In benzene at 60℃; for 24h; Further byproducts given; | A 23% B 23% C 6% D 6% |
diisopropyl peroxydicarbonate
A
triphenylmethyl alcohol
B
2-(4-chlorophenyl)benzoxazole
C
triphenylmethyl iso-propyl ether
Conditions | Yield |
---|---|
In benzene at 60℃; for 24h; Product distribution; Mechanism; | A 23% B 23% C 6% D 6% E 3% |
diisopropyl peroxydicarbonate
C
2-(4-methoxyphenyl)-1-phenyl-1H-benzo[d]imidazole
Conditions | Yield |
---|---|
In benzene at 60℃; for 18h; | A 18% B 21% C 13% |
diisopropyl peroxydicarbonate
phenylacetylene
A
(1-isopropoxyethyl)benzene
B
1-Phenylethanol
Conditions | Yield |
---|---|
In benzene at 60℃; Product distribution; Mechanism; same produts were determined by GC; | A n/a B n/a C 21% D n/a E n/a F n/a |
diisopropyl peroxydicarbonate
(E)-N-benzylidenebenzenamine
A
Benzoyl-phenyl-carbamic acid isopropyl ester
B
2-phenyl-4-(trimethylsilyl)quinoline
Conditions | Yield |
---|---|
With ethenyltrimethylsilane In benzene at 60℃; for 4h; | A 20% B 7% |
diisopropyl peroxydicarbonate
A
1,2-diphenyl-1H-benzoimidazole
C
1,3-diphenyl-1H-quinoxalin-2-one
Conditions | Yield |
---|---|
In benzene at 60℃; for 30h; | A 20% B 14% C 14% |
diisopropyl peroxydicarbonate
A
4-Methoxybenzophenone
B
4-methoxy-benzaldehyde
C
11-(4-methoxyphenyl)dibenz<1,4>oxazepine
Conditions | Yield |
---|---|
In benzene at 60℃; for 6h; imine:reagent=1:4; Yield given. Further byproducts given; | A 18% B n/a C 17% D n/a |
Chemical Name: Diisopropyl peroxydicarbonate
IUPAC NAME: Propan-2-yl propan-2-yloxycarbonyloxy carbonate
CAS No.: 105-64-6
EINECS: 203-317-4
RTECS Class: Primary Irritant
Molecular Formula: C8H14O6
Molecular Weight: 206.19 g/mol
Melting Point: 12°C
Density: 1.138 g/cm3
Flash Point: 79.1 °C
Boiling Point: 208 °C at 760 mmHg
Sensitive: Heat sensitive.
Following is the structure of Diisopropyl perdicarbonate (105-64-6):
The chemical synonymous of Diisopropyl perdicarbonate (105-64-6) are Diisopropyl peroxydicarbonate ; Bisisopropyl peroxydicarbonate ; Isopropyl peroxydicarbonate ; Isopropyl peroxycarbonate ; Peroxydicarbonic acid, diisopropyl ester ; Isopropylpercarbonate ; Diisopropylperoxydicarbonat ; Diisopropyl peroxydiformate
1. | eye-rbt 500 mg SEV | IHFCAY Industrial Hygiene Foundation of America, Chemical and Toxicological Series, Bulletin. 6 (1967),1. | ||
2. | orl-rat LD50:2140 mg/kg | IHFCAY Industrial Hygiene Foundation of America, Chemical and Toxicological Series, Bulletin. 6 (1967),1. | ||
3. | skn-rbt LD50:2025 mg/kg | BSPII* SPI Bulletin. (Society of the Plastics Industry, 250 Park Ave., New York, NY 10017) 1/75-19B . |
Reported in EPA TSCA Inventory.
Moderately toxic by ingestion and skin contact. A severe eye irritant. Very dangerous fire hazard. Dangerously unstable above 10°C. An impact- and heat-sensitive explosive. Solutions may spontaneously explode (the hazard increases with concentration). Storage in sealed containers may be dangerous. Explodes on contact with amines or potassium iodide. May explode on contact with organic matter. When heated to decomposition it emits acrid smoke and fumes. See also PEROXIDES, ORGANIC.
Attention:
1. Storage: Keep in a cool, dry, dark location in a tightly sealed container or cylinder. Keep away from incompatible materials, ignition sources and untrained individuals. Secure and label area. Protect containers/cylinders from physical damage.
2. Handling: All chemicals should be considered hazardous. Avoid direct physical contact. Use appropriate, approved safety equipment. Untrained individuals should not handle this chemical or its container. Handling should occur in a chemical fume hood.
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